Evidence map›Paper›PMID 29132243›Full record

ArticleJournal of neurotrauma2018

Protective Effects of Estradiol and Dihydrotestosterone following Spinal Cord Injury.

Dale R Sengelaub, Qi Han, Nai-Kui Liu, Melissa A Maczuga, Violetta Szalavari, Stephanie A Valencia, Xiao-Ming Xu

Open access · greenAbstract read
In one paragraph

Article in Journal of neurotrauma, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Dale R Sengelaub1 Psychological and Brain Sciences, Indiana University , Bloomington, Indiana.
Qi Han2 Department of Neurological Surgery, Indiana University School of Medicine , Indianapolis, Indiana.
Nai-Kui Liu2 Department of Neurological Surgery, Indiana University School of Medicine , Indianapolis, Indiana.
Melissa A Maczuga1 Psychological and Brain Sciences, Indiana University , Bloomington, Indiana.
Violetta Szalavari1 Psychological and Brain Sciences, Indiana University , Bloomington, Indiana.
Stephanie A Valencia1 Psychological and Brain Sciences, Indiana University , Bloomington, Indiana.
Xiao-Ming Xu3 Spinal Cord and Brain Injury Research Group, Indiana University School of Medicine , Indianapolis, Indiana.
Indiana University Bloomington · USIndiana University – Purdue University Indianapolis · USNeurological Surgery · US

Funding

Reprogramming reactive glial cells into functional new neurons after SCIR01NS111776 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI WU, WEI, ZHANG, CHUN-LI · 2020 to 2024
$2.4M
Cardiolipin as a Novel Target for Neuroprotection after Spinal Cord InjuryI01BX003705 · VA · RLR VA MEDICAL CENTER · PI XU, XIAO-MING · 2018 to 2021
–
BLRD VA I01 BX003705NINDS NIH HHS R01 NS111776
6 · The paper itself

Abstract

Spinal cord injury (SCI) results in lesions that destroy tissue and disrupt spinal tracts, producing deficits in locomotor and autonomic function. We previously demonstrated that motoneurons and the muscles they innervate show pronounced atrophy after SCI, and these changes are prevented by treatment with testosterone. Here, we assessed whether the testosterone active metabolites estradiol and dihydrotestosterone have similar protective effects after SCI. Young adult female rats received either sham or T9 spinal cord contusion injuries and were treated with estradiol, dihydrotestosterone, both, or nothing via Silastic capsules. Basso-Beattie-Bresnahan locomotor testing was performed weekly and voiding behavior was assessed at 3 weeks post-injury. Four weeks after SCI, lesion volume and tissue sparing, quadriceps muscle fiber cross-sectional area, and motoneuron dendritic morphology were assessed. Spontaneous locomotor behavior improved after SCI, but hormone treatments had no effect. Voiding behavior was disrupted after SCI, but was significantly improved by treatment with either estradiol or dihydrotestosterone; combined treatment was maximally effective. Treatment with estradiol reduced lesion volume, but dihydrotestosterone alone and estradiol combined with dihydrotestosterone were ineffective. SCI-induced decreases in motoneuron dendritic length were attenuated by all hormone treatments. SCI-induced reductions in muscle fiber cross-sectional areas were prevented by treatment with either dihydrotestosterone or estradiol combined with dihydrotestosterone, but estradiol treatment was ineffective. These findings suggest that deficits in micturition and regressive changes in motoneuron and muscle morphology seen after SCI are ameliorated by treatment with estradiol or dihydrotestosterone, further supporting a role for steroid hormones as neurotherapeutic agents in the injured nervous system.

Indexed as

AnimalsDihydrotestosteroneEstradiolFemaleLocomotionMotor NeuronsMuscle, SkeletalRatsRats, Sprague-DawleyRecovery of FunctionSpinal Cord InjuriesDihydrotestosteroneEstradioldendritesmorphologyneuroprotectionsteroids

Identifiers

PMID29132243
PMCPMC5863086
OpenAlexW2770337890

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.